MagnetOs Putty
K-Number: K181958 · 2018-12-06
ApplicantKuros Biosciences B.V
Decision Date2018-12-06
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MagnetOs Putty is a medical device manufactured by Kuros Biosciences B.V. It received FDA 510(k) clearance on 2018-12-06 under approval number K181958. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MagnetOs Putty?
MagnetOs Putty is a medical device that received FDA 510(k) clearance on 2018-12-06. It is manufactured by Kuros Biosciences B.V. The 510(k) number is K181958.
When was MagnetOs Putty approved by the FDA?
MagnetOs Putty received FDA 510(k) clearance on 2018-12-06, under approval number K181958.
What company makes MagnetOs Putty?
MagnetOs Putty is manufactured by Kuros Biosciences B.V.
What is the FDA product code for MagnetOs Putty?
The FDA product code for MagnetOs Putty is MQV.
Related Clinical Trials
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A Prospective, Randomized, Single-blind, Controlled, Multi-center Study to Assess the Safety and Performance of MagnetOsTM Compared to Autogenous Bone Graft in Patients Undergoing Hindfoot or Ankle Fusions.
RECRUITING
NCT07512336
A Randomized Intra-Patient Controlled Trial of MagnetOs™ Putty vs Autograft in Instrumented Posterolateral Spinal Fusion in Idiopathic Scoliosis Patients
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Other Devices by Kuros Biosciences B.V
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.